Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs4149570
TNFRSF1A
0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs1085308054
PTEN
0.827 0.160 10 87952231 frameshift variant AT/- delins 7
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs121434257
AIRE
0.827 0.080 21 44289686 missense variant G/A;T snv 4.0E-05 6
rs2160322
MAGI2
0.851 0.160 7 78462650 intron variant G/A;C snv 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4